2013
DOI: 10.1016/j.molliq.2013.05.011
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Efficient deep eutectic solvents catalyzed synthesis of pyran and benzopyran derivatives

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Cited by 103 publications
(35 citation statements)
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“…In continuation of our efforts to develop environmentally benign solvents and catalysts for useful organic transformations, herein, we report a very effective and green procedure for the one‐pot synthesis of diverse racemic α‐aminonitriles in excellent yields using magnetic g‐C 3 N 4 as an inexpensive and environmentally benign catalyst under mild conditions. The presented method not only uses a cost‐effective and magnetically recoverable catalyst and environmentally benign solvent, but also experimentally safe and easy‐to‐handle TMSCN as reagent.…”
Section: Resultsmentioning
confidence: 99%
“…In continuation of our efforts to develop environmentally benign solvents and catalysts for useful organic transformations, herein, we report a very effective and green procedure for the one‐pot synthesis of diverse racemic α‐aminonitriles in excellent yields using magnetic g‐C 3 N 4 as an inexpensive and environmentally benign catalyst under mild conditions. The presented method not only uses a cost‐effective and magnetically recoverable catalyst and environmentally benign solvent, but also experimentally safe and easy‐to‐handle TMSCN as reagent.…”
Section: Resultsmentioning
confidence: 99%
“…Likewise, the same 1:2 ChCl/urea (molar ratio) DES was used as the catalyst and solvent to afford benzopyran and pyran derivatives by the one‐pot three‐component reaction of 1,3‐dicarbonyl compounds (acetyl acetone, ethyl acetoacetate, and dimedone), aromatic aldehydes, and malononitrile (Scheme ) . The reactions were performed at 80 °C and rendered high isolated yields (75–95 %).…”
Section: Des In Organocatalysis: Reactive Basic or Acidic Solvents Fomentioning
confidence: 99%
“… Synthesis of pyran and benzopyran derivatives in DES using different aldehydes, malonitrile, and 1,3‐dicarbonyl compounds …”
Section: Des In Organocatalysis: Reactive Basic or Acidic Solvents Fomentioning
confidence: 99%
“…The ease of preparation, availability, cost effectiveness, stability, less toxicity, and biodegradability make these DESs versatile alternatives to ionic liquids. In view of some previous works [26][27][28][29][30][31][32][33][34][35][36][37][38] and our recent research programme on the development of novel and environmentally benign synthetic methodologies [39][40][41][42][43][44][45], herein we report ChCl/itaconic acid as reaction medium and catalyst for the synthesis of 13-aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones by condensation of 2-hydroxynaphthalene-1,4-dione with aldehydes (Scheme 1).…”
Section: Introductionmentioning
confidence: 99%